Hentriacontane-5,14,16-trione

Details

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Internal ID 73d283f9-f829-4724-85f4-e747bcb7e61d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > 1,3-dicarbonyl compounds > Beta-diketones
IUPAC Name hentriacontane-5,14,16-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H58O3/c1-3-5-7-8-9-10-11-12-13-14-15-19-22-26-30(33)28-31(34)27-23-20-17-16-18-21-25-29(32)24-6-4-2/h3-28H2,1-2H3
InChI Key FJTRXLCXEVTOSC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H58O3
Molecular Weight 478.80 g/mol
Exact Mass 478.43859571 g/mol
Topological Polar Surface Area (TPSA) 51.20 Ų
XlogP 11.00
Atomic LogP (AlogP) 9.88
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 28

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hentriacontane-5,14,16-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 - 0.6188 61.88%
Blood Brain Barrier + 0.8080 80.80%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7231 72.31%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9325 93.25%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8566 85.66%
P-glycoprotein inhibitior - 0.4855 48.55%
P-glycoprotein substrate - 0.8700 87.00%
CYP3A4 substrate - 0.6702 67.02%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7781 77.81%
CYP3A4 inhibition - 0.9521 95.21%
CYP2C9 inhibition - 0.8894 88.94%
CYP2C19 inhibition - 0.9249 92.49%
CYP2D6 inhibition - 0.9289 92.89%
CYP1A2 inhibition - 0.5785 57.85%
CYP2C8 inhibition - 0.9630 96.30%
CYP inhibitory promiscuity - 0.9079 90.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6323 63.23%
Carcinogenicity (trinary) Non-required 0.7279 72.79%
Eye corrosion + 0.9333 93.33%
Eye irritation + 0.9177 91.77%
Skin irritation - 0.5505 55.05%
Skin corrosion - 0.7436 74.36%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5959 59.59%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6924 69.24%
skin sensitisation - 0.8236 82.36%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.8425 84.25%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5863 58.63%
Acute Oral Toxicity (c) II 0.4484 44.84%
Estrogen receptor binding - 0.6302 63.02%
Androgen receptor binding - 0.8656 86.56%
Thyroid receptor binding + 0.5304 53.04%
Glucocorticoid receptor binding - 0.6447 64.47%
Aromatase binding - 0.7069 70.69%
PPAR gamma - 0.4918 49.18%
Honey bee toxicity - 0.9926 99.26%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.8238 82.38%
Fish aquatic toxicity + 0.8920 89.20%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.81% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.66% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.65% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.13% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.67% 95.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.37% 97.29%
CHEMBL230 P35354 Cyclooxygenase-2 88.88% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.56% 92.86%
CHEMBL299 P17252 Protein kinase C alpha 84.29% 98.03%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.00% 94.33%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.97% 85.94%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.47% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.51% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Poa secunda subsp. juncifolia

Cross-Links

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PubChem 162998231
LOTUS LTS0050245
wikiData Q104996335